Polyendocrinopathies, Autoimmune
"Polyendocrinopathies, Autoimmune" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Autoimmune diseases affecting multiple endocrine organs. Type I is characterized by childhood onset and chronic mucocutaneous candidiasis (CANDIDIASIS, CHRONIC MUCOCUTANEOUS), while type II exhibits any combination of adrenal insufficiency (ADDISON'S DISEASE), lymphocytic thyroiditis (THYROIDITIS, AUTOIMMUNE;), HYPOPARATHYROIDISM; and gonadal failure. In both types organ-specific ANTIBODIES against a variety of ENDOCRINE GLANDS have been detected. The type II syndrome differs from type I in that it is associated with HLA-A1 and B8 haplotypes, onset is usually in adulthood, and candidiasis is not present.
Descriptor ID |
D016884
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MeSH Number(s) |
C19.787 C20.111.750
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Concept/Terms |
Polyglandular Type III Autoimmune Syndrome- Polyglandular Type III Autoimmune Syndrome
- Polyglandular Autoimmune Syndrome, Type 3
- Autoimmune Syndrome Type III, Polyglandular
- Autoimmune Polyglandular Syndrome Type III
- Autoimmune Polyglandular Syndrome, Type 3
Polyglandular Type I Autoimmune Syndrome- Polyglandular Type I Autoimmune Syndrome
- APECED
- APS Type 1
- Autoimmune Polyendocrinopathy Syndrome Type 1
- Autoimmune Polyendocrinopathy with Candidiasis and Ectodermal Dystrophy
- Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy
- Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy
- Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, Autoimmune
- Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy
- Autoimmune Polyglandular Syndrome Type I
- Autoimmune Polyglandular Syndrome, Type 1
- Autoimmune Polyglandular Syndrome, Type I
- Autoimmune Syndrome Type I, Polyglandular
- Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy, Autoimmune
- Polyendocrinopathy Candidiasis Ectodermal Dystrophy, Autoimmune
- Polyglandular Autoimmune Syndrome, Type 1
- Polyglandular Autoimmune Syndrome, Type I
- AIRE Deficiency
- AIRE Deficiencies
- Deficiency, AIRE
Polyglandular Type II Autoimmune Syndrome- Polyglandular Type II Autoimmune Syndrome
- Autoimmune Polyendocrine Syndrome, Type II
- Autoimmune Polyglandular Syndrome Type II
- Autoimmune Syndrome Type II, Polyglandular
- Diabetes Mellitus, Addison Disease, Myxedema
- Schmidt's Syndrome
- Syndrome, Schmidt's
- Multiple Endocrine Deficiency Syndrome, Type 2
- Polyendocrine Autoimmune Syndrome, Type II
- Polyglandular Autoimmune Syndrome, Type 2
- Polyglandular Deficiency Syndrome, Type 2
- Schmidt Syndrome
- Syndrome, Schmidt
- Autoimmune Polyendocrine Syndrome, Type 2
- Diabetes Mellitus, Addison's Disease, Myxedema
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Below are MeSH descriptors whose meaning is more general than "Polyendocrinopathies, Autoimmune".
Below are MeSH descriptors whose meaning is more specific than "Polyendocrinopathies, Autoimmune".
This graph shows the total number of publications written about "Polyendocrinopathies, Autoimmune" by people in this website by year, and whether "Polyendocrinopathies, Autoimmune" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2007 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2009 | 0 | 1 | 1 |
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Below are the most recent publications written about "Polyendocrinopathies, Autoimmune" by people in Profiles.
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Ohsie S, Gerney G, Gui D, Kahana D, Mart?n MG, Cortina G. A paucity of colonic enteroendocrine and/or enterochromaffin cells characterizes a subset of patients with chronic unexplained diarrhea/malabsorption. Hum Pathol. 2009 Jul; 40(7):1006-14.
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Yong PL, Russo P, Sullivan KE. Use of sirolimus in IPEX and IPEX-like children. J Clin Immunol. 2008 Sep; 28(5):581-7.
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Heltzer ML, Choi JK, Ochs HD, Sullivan KE, Torgerson TR, Ernst LM. A potential screening tool for IPEX syndrome. Pediatr Dev Pathol. 2007 Mar-Apr; 10(2):98-105.